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Clinical and Supply Chain Integration

Most of the pharmaceutical and Biotech companies use multiple Clinical Research Organizations (CROs) for the clinical trial management. Due to lack of advanced technologies in the third world, IVR systems are used to manage dispensing drugs to patients. Every clinical trial is custom developed and validated hence resulting in time and productivity loss. Most of the time CROs and their life science clients work in silos.

Data exchange is done either manually or via email thus resulting in redundancy and productivity loss.

Life Science companies can achieve significant ROI in terms of increase in productivity and reduction in time if they integrate their internal applications (such as trial management, clinical data management, supply chain) with CRO applications.

LGS offers XML based open architecture that standardizes the data communication between the internal and external systems and hence reduces the clinical study setup, increases the productivity and data reliability.

Significant benefits include:

bullet More efficient trial management by standardized initiation and ongoing activities
bullet Closer partnership with investigative sites
bullet Reduction in manual manipulation of data by seamless real-time electronic data exchange
bullet Potential time saving of 5-8 weeks in IVRS study, setup by using template based simple and standardized development and validation process
bullet Standardized user training resulting in reduction of learning curve
bullet Real-time inventory dashboard for investigation sites
 
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